International Journal of Medical Sciences · 2014 · 65 citations · 21 references
MedicineMolecular GeneticsPharmacologyMedical GeneticsPharmacogeneticsPharmacogenomicsCytochrome P450 EnzymesCytochrome P450-mediated MetabolismDrug Metabolism GeneticsPharmacogenetic TestingPopulation PharmacogeneticsCommon Genetic VariantsCyp2c9 GenotypingCyp3a5 GenotypingCyp3a5 PharmacogeneticsCytochrome P450 Genetic PolymorphismCytochrome P450 GenotypingDrug-metabolizing Enzyme VariabilityGenetic Polymorphisms
The Cytochrome P450 is the major enzyme involved in drug metabolism. CYP enzymes are responsible for the metabolism of most clinically used drugs. Individual variability in CYP activity is one important factor that contributes to drug therapy failure. We have developed a new straightforward TaqMan PCR genotyping assay to investigate the prevalence of the most common allelic variants of polymorphic CYP enzymes CYP1A2, CYP2C9, CYP2C19, CYP2D6 and CYP3A5 in the Japanese population. Moreover, we focused on the combination of each genotype for clinical treatment. The genotype analysis identified a total of 139 out of 483 genotype combinations of five genes in the 1,003 Japanese subjects. According to our results, most of subjects seemed to require dose modification during clinical treatment. In the near future, modifications should be considered based on the individual patient genotype of each treatment.
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Kristine R. Crews, Andrea Gaedigk, Henry M. Dunnenberger et al. · Clinical Pharmacology & Therapeutics · 2011 · 368 citations · Full text
S P Myrand, Kanako Sekiguchi, MZ Man et al. · Clinical Pharmacology & Therapeutics · 2008 · 225 citations